As a post-doctoral fellow in molecular genetics, Dr. Patrick Gaffney has played a major role in a large scale collaborative project between the Institute of Human Genetics and Department of Medicine which seeks to identify susceptibility loci within the human genome for systemic lupus erythematosus (SLE). The hypothesis driving these studies is that SLE is a complex genetic disease, with inheritance of a few genes conferring susceptibility. Our laboratory has recently completed a genome screen in 105 SLE sib pair families, and has identified potential susceptibility intervals on chromosomes 6, 14, 16, and 20.
The aim of the current proposal is to examine the region on chromosome 20 in detail, using a large collection of sib pairs with SLE and their available parents. Evidence for linkage to chromosome 20 has also been demonstrated in an independent cohort of multiplex families by our colleagues at the Oklahoma Medical Research Foundation (OMRF) making this chromosome highly attractive for further fine-mapping efforts. Highly informative short tandem repeat polymorphisms (STRPs) will be utilized to confirm linkage and subsequently narrow the region of interest. When linkage is confirmed and further refined, potential candidate genes in the area will be screened by direct sequencing for mutations or polymorphisms. If the candidate gene effort is not fruitful, we will proceed with construction of a physical map of the region and isolation of novel genes. The long term goal of this project is to identify genes that confer susceptibility to SLE, which should provide a framework for understanding the etiology of the disease and subsequently developing novel effective treatments. Dr. Gaffney's career goal is to be an independent academic physician-scientist. Dr. Tim Behrens, the proposed sponsor, has extensive experience in molecular biology and immunology and has a special interest in the genetics of SLE. The co-sponsors of this proposal, Drs. Dick King and Steve Rich, will provide expertise in the molecular genetics of complex disease and in genetic statistical analysis. The academic milieu at the University of Minnesota, together with the assembled group of sponsors, will provide the high quality training environment necessary for Dr. Gaffney's development into an independent investigator.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08AR002105-05
Application #
6632609
Study Section
Arthritis and Musculoskeletal and Skin Diseases Special Grants Review Committee (AMS)
Program Officer
Serrate-Sztein, Susana
Project Start
1999-07-01
Project End
2004-10-31
Budget Start
2003-07-01
Budget End
2004-10-31
Support Year
5
Fiscal Year
2003
Total Cost
$125,280
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
555917996
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Graham, Robert R; Cotsapas, Chris; Davies, Leela et al. (2008) Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus. Nat Genet :
Graham, Robert R; Cotsapas, Chris; Davies, Leela et al. (2008) Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus. Nat Genet 40:1059-61
Gaffney, Patrick M; Langefeld, Carl D; Graham, Robert R et al. (2006) Fine-mapping chromosome 20 in 230 systemic lupus erythematosus sib pair and multiplex families: evidence for genetic epistasis with chromosome 16q12. Am J Hum Genet 78:747-58
Gaffney, P M; Ortmann, W A; Selby, S A et al. (2000) Genome screening in human systemic lupus erythematosus: results from a second Minnesota cohort and combined analyses of 187 sib-pair families. Am J Hum Genet 66:547-56